Evidence map›Paper›PMID 39746995›Full record

ArticleNature communications2025

DSIF factor Spt5 coordinates transcription, maturation and exoribonucleolysis of RNA polymerase II transcripts.

Krzysztof Kuś, Loic Carrique, Tea Kecman, Marjorie Fournier, Sarah Sayed Hassanein, Ebru Aydin, Cornelia Kilchert, Jonathan M Grimes, Lidia Vasiljeva

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
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  9. Review
  10. Toward structural understanding of eukaryotic transcription elongation.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2025
    Review
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Krzysztof KuśDepartment of Biochemistry, University of Oxford, Oxford, United Kingdom. krzysztof.kus@bioch.ox.ac.uk.ORCID 0000-0003-4791-9658
Loic CarriqueDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-5332-8593
Tea KecmanDepartment of Biochemistry, University of Oxford, Oxford, United Kingdom.
Marjorie FournierDepartment of Biochemistry, University of Oxford, Oxford, United Kingdom.
Sarah Sayed HassaneinDepartment of Biochemistry, University of Oxford, Oxford, United Kingdom.
Ebru AydinInstitut für Biochemie, Justus-Liebig-Universität Gießen, Gießen, Germany.ORCID 0009-0007-8992-4259
Cornelia KilchertInstitut für Biochemie, Justus-Liebig-Universität Gießen, Gießen, Germany.ORCID 0000-0001-6834-0704
Jonathan M GrimesDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-9698-0389
Lidia VasiljevaDepartment of Biochemistry, University of Oxford, Oxford, United Kingdom. lidia.vasilieva@bioch.ox.ac.uk.ORCID 0000-0002-1244-8772

Funding

RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/Y00194X/1Wellcome Trust 222510Wellcome Trust (Wellcome) WT106994/Z/15/Z
6 · The paper itself

Abstract

Precursor messenger RNA (pre-mRNA) is processed into its functional form during RNA polymerase II (Pol II) transcription. Although functional coupling between transcription and pre-mRNA processing is established, the underlying mechanisms are not fully understood. We show that the key transcription termination factor, RNA exonuclease Xrn2 engages with Pol II forming a stable complex. Xrn2 activity is stimulated by Spt5 to ensure efficient degradation of nascent RNA leading to Pol II dislodgement from DNA. Our results support a model where Xrn2 first forms a stable complex with the elongating Pol II to achieve its full activity in degrading nascent RNA revising the current 'torpedo' model of termination, which posits that RNA degradation precedes Xrn2 engagement with Pol II. Spt5 is also a key factor that attenuates the expression of non-coding transcripts, coordinates pre-mRNA splicing and 3'-end processing. Our findings indicate that engagement with the transcribing Pol II is an essential regulatory step modulating the activity of RNA enzymes such as Xrn2, thus advancing our understanding of how RNA maturation is controlled during transcription.

Indexed as

ExoribonucleasesRNA Polymerase IITranscriptional Elongation FactorsTranscription, GeneticChromosomal Proteins, Non-HistoneHumansRNA, MessengerRNA PrecursorsRNA SplicingRNA StabilityChromosomal Proteins, Non-HistoneExoribonucleasesRNA, MessengerRNA Polymerase IIRNA PrecursorsSPT5 transcriptional elongation factorTranscriptional Elongation FactorsXRN2 protein, human

Identifiers

PMID39746995
PMCPMC11695829

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.